Hemodialysis
A machine filters your blood outside the body, usually three times a week at a dialysis center, or at home.
Understanding your illness takes away some of the fear of the unknown. Here are the words you will hear, and the choices you have.

Most people have two kidneys, each about the size of a fist, just below the rib cage on either side of the spine.
Kidneys also help control blood pressure, keep your bones strong, and tell your body to make red blood cells. When kidneys are damaged, waste and fluid build up, which is why people with kidney failure need dialysis or a transplant to do this work for them.
Doctors use a blood test called eGFR to measure how well your kidneys filter. The higher the number, the better. Kidney disease is grouped into five stages. Many people live for years in the early stages, especially when diabetes and blood pressure are well controlled.
There is more than one way to treat kidney failure. Talk with your care team about which fits your health, home and daily life.
Usually done at a dialysis center three times a week, about four hours each time. Some people do it at home.
Done at home every day. The lining of your belly, called the peritoneum, works as the filter.
A machine filters your blood outside the body, usually three times a week at a dialysis center, or at home.
Continuous ambulatory peritoneal dialysis. The lining of your belly filters your blood. You change the fluid by hand several times a day.
Continuous cycling peritoneal dialysis. A machine changes the fluid for you at night while you sleep.
A healthy kidney from a living or deceased donor takes over the work. Your care team can explain whether you are eligible.
An access is the place on your body where blood is taken out and returned during hemodialysis. It is usually made with a small surgery weeks or months before you start.
A surgeon joins an artery and a vein, usually in your arm. It needs time to heal before use, but it tends to last longest and has fewer infections.
A soft tube connects an artery and a vein. It can be used sooner than a fistula, and is an option when veins are small.
A tube placed in a large vein, often in the neck or chest. It is usually used for a short time while a fistula or graft heals.
Small daily habits make a big difference. Your dietitian and care team will give you limits that are right for you.
Skipping or shortening dialysis lets waste and fluid build up quickly. If you feel unwell or cannot make a session, call your dialysis center right away.
Your care team will tell you how much to drink each day. Anything liquid at room temperature counts, including soup, ice and gelatin.
Less salt means less thirst, easier fluid control and better blood pressure. Fresh foods usually have less salt than canned or packaged ones.
Ask what your lab results mean. Your dietitian can show you which foods to limit, and if you take a phosphate binder, take it with meals as prescribed.
Keep your access clean, check it every day as your care team showed you, and do not allow blood pressure cuffs, tight sleeves or needles on that arm.
Gentle activity that your doctor approves helps your energy and mood. Talking with others who understand, like at our Hang-Out, helps too.
Short videos for anyone just starting out. Watch them with your family.
A short introduction for anyone newly diagnosed.
What happens before, during and after a hemodialysis session.
How exchanges work and what a day on PD looks like.
Anyone can develop kidney disease, but the risk is higher if you have diabetes, high blood pressure, heart disease, or a family history of kidney failure. African Americans are more likely to develop kidney disease because of diabetes and hypertension. Early kidney disease often has no symptoms, so a simple blood and urine test is the best way to find it early.
Early screening is the key to prevention.
Want to learn more? See our helpful links to trusted kidney organizations, or bring your questions to our monthly meeting.
This information is for education only and is not medical advice. Always talk with your doctor, nurse or dialysis care team about your own health and treatment.